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3-(4-chlorobenzyl)piperidine-2,6-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24866-79-3

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24866-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24866-79-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,8,6 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24866-79:
(7*2)+(6*4)+(5*8)+(4*6)+(3*6)+(2*7)+(1*9)=143
143 % 10 = 3
So 24866-79-3 is a valid CAS Registry Number.

24866-79-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(4-chlorophenyl)methyl]piperidine-2,6-dione

1.2 Other means of identification

Product number -
Other names 2-(p-Chlorobenzyl)glutarimide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:24866-79-3 SDS

24866-79-3Relevant academic research and scientific papers

Transition-metal-based Lewis acid and base ambiphilic catalysts of iridium hydride complexes: Multicomponent synthesis of glutarimides

Takaya, Hikaru,Yoshida, Kazunori,Isozaki, Katsuhiro,Terai, Hiroki,Murahashi, Shun-Ichi

, p. 3302 - 3304 (2007/10/03)

Mutual destruction of reagents in acid-and base-promoted reactions in the same container is now avoidable with the iridium polyhydride complex [IrH5(PiPr3)2] (1), which is an ambiphilic Lewis acid and base catalyst. By using catalyst 1, a three-component reaction of nitriles, olefins, and water proceeds efficiently to give glutarimides, which are pharmacologically important (see scheme).

Synthesis and anticonvulsant activity of 2-benzylglutarimides

Goehring,Greenwood,Nwokogu,Pisipati,Rogers,Wolfe

, p. 926 - 931 (2007/10/02)

A series of 2-benzylglutarimides (4) and their N-methyl analogues (5) were prepared according to the Topliss scheme for the selection of benzyl substituents to maximize anticonvulsant activity. A total of 22 such compounds were subjected to initial (phase

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